Haemonetics Corporation said the U.S. Food and Drug Administration granted 510(k) clearance for the NexSys PCS Plasma Collection System with Persona PLUS technology. The company stated the clearance was supported by clinical data from a prospective, randomized, controlled, multicenter pivotal trial involving more than 30,000 plasma donations from nearly 3,000 donors, and that the system increased average plasma volume per donation by a mid-single digit percentage compared with the prior Persona technology.
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